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EZH2: biology, disease, and structure-based drug discovery

EZH2 is the catalytic subunit of the polycomb repressive complex 2 (PRC2), which is a highly conserved histone methyltransferase that methylates lysine 27 of histone 3. Overexpression of EZH2 has been found in a wide range of cancers, including those of the prostate and breast. In this review, we ad...

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Autores principales: Tan, Jin-zhi, Yan, Yan, Wang, Xiao-xi, Jiang, Yi, Xu, H Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914023/
https://www.ncbi.nlm.nih.gov/pubmed/24362326
http://dx.doi.org/10.1038/aps.2013.161
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author Tan, Jin-zhi
Yan, Yan
Wang, Xiao-xi
Jiang, Yi
Xu, H Eric
author_facet Tan, Jin-zhi
Yan, Yan
Wang, Xiao-xi
Jiang, Yi
Xu, H Eric
author_sort Tan, Jin-zhi
collection PubMed
description EZH2 is the catalytic subunit of the polycomb repressive complex 2 (PRC2), which is a highly conserved histone methyltransferase that methylates lysine 27 of histone 3. Overexpression of EZH2 has been found in a wide range of cancers, including those of the prostate and breast. In this review, we address the current understanding of the oncogenic role of EZH2, including its PRC2-dependent transcriptional repression and PRC2-independent gene activation. We also discuss the connections between EZH2 and other silencing enzymes, such as DNA methyltransferase and histone deacetylase. We comprehensively address the architecture of the PRC2 complex and the crucial roles of each subunit. Finally, we summarize new progress in developing EZH2 inhibitors, which could be a new epigenetic therapy for cancers.
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spelling pubmed-39140232014-02-05 EZH2: biology, disease, and structure-based drug discovery Tan, Jin-zhi Yan, Yan Wang, Xiao-xi Jiang, Yi Xu, H Eric Acta Pharmacol Sin Review EZH2 is the catalytic subunit of the polycomb repressive complex 2 (PRC2), which is a highly conserved histone methyltransferase that methylates lysine 27 of histone 3. Overexpression of EZH2 has been found in a wide range of cancers, including those of the prostate and breast. In this review, we address the current understanding of the oncogenic role of EZH2, including its PRC2-dependent transcriptional repression and PRC2-independent gene activation. We also discuss the connections between EZH2 and other silencing enzymes, such as DNA methyltransferase and histone deacetylase. We comprehensively address the architecture of the PRC2 complex and the crucial roles of each subunit. Finally, we summarize new progress in developing EZH2 inhibitors, which could be a new epigenetic therapy for cancers. Nature Publishing Group 2014-02 2013-12-23 /pmc/articles/PMC3914023/ /pubmed/24362326 http://dx.doi.org/10.1038/aps.2013.161 Text en Copyright © 2014 CPS and SIMM http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Review
Tan, Jin-zhi
Yan, Yan
Wang, Xiao-xi
Jiang, Yi
Xu, H Eric
EZH2: biology, disease, and structure-based drug discovery
title EZH2: biology, disease, and structure-based drug discovery
title_full EZH2: biology, disease, and structure-based drug discovery
title_fullStr EZH2: biology, disease, and structure-based drug discovery
title_full_unstemmed EZH2: biology, disease, and structure-based drug discovery
title_short EZH2: biology, disease, and structure-based drug discovery
title_sort ezh2: biology, disease, and structure-based drug discovery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914023/
https://www.ncbi.nlm.nih.gov/pubmed/24362326
http://dx.doi.org/10.1038/aps.2013.161
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